Isolating cells from adult murine brain for validation of cell-type specific cre-mediated deletion.

J Neurosci Methods

Centre for Molecular Medicine and Therapeutics, Department of Medical Genetics, University of British Columbia and Children's and Women's Hospital, 980 West 28thAvenue, Vancouver, BC, V5Z 4H4, Canada; Division of Neurology, Department of Medicine, University of British Columbia Hospital, S 192-2211 Wesbrook Mall, Vancouver, BC, V6T 2B5, Canada; Brain Research Center, University of British Columbia, Vancouver, BC, V6T 1Z3, Canada. Electronic address:

Published: December 2019

Background: TheCre/loxP system allows for the temporal and spatial investigation of the expression of a single gene in the nervous system. Current methods of validating conditional knock-out mouse models rely on heterogeneous brain tissue or primary culture. These methods may assess the extent of genetic knockdown in the brain but do not provide age-appropriate, cell-type specific information.

New Method: We isolated specific cell types from adult murine brain using FACS to assess cell type-specific gene expression in conditional mouse models.

Results: We identified robust but incomplete genetic knockdown in microglia isolated from two separate microglia-specific knockout models.

Comparisonwith Existing Methods(s): Genetic knockdown in isolated adult microglia differed significantly from cultured primary microglia.

Conclusions: Differences observed in primary cultured microglia compared to isolated adult microglia suggest that current methods used to validate microglia-specific gene deletion over-estimate deletion efficiency. Assessment of gene expression in isolated adult microglia provides a more accurate assessment of Cre-mediated gene deletion.

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http://dx.doi.org/10.1016/j.jneumeth.2019.108422DOI Listing

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